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用于评估神经保护化合物的嗜铬细胞细胞毒性模型。

Cytotoxicity Models in Chromaffin Cells to Evaluate Neuroprotective Compounds.

机构信息

Instituto Teófilo Hernando. Departamento de Farmacología. Facultad de Medicina. Universidad Autónoma de Madrid and Instituto de investigación Sanitaria Hospital de la Princesa, Madrid, Spain.

出版信息

Methods Mol Biol. 2023;2565:361-370. doi: 10.1007/978-1-0716-2671-9_24.

Abstract

Primary cultures of bovine chromaffin cells are considered a good model to evaluate potential neuroprotective compounds for two major reasons: (i) they share many common features to neurons as they synthesize, store, and release neurotransmitters; they are excitable cells that express voltage-dependent calcium, potassium, and sodium channels; they express different neuronal receptor subtypes; and (ii) they can be easily cultured in high quantities from adult animals; as adult para-neurons, they can be used to reproduce different neurodegenerative-like cytotoxicity models. In this chapter, we describe protocols to mimic calcium overload (veratridine and thapsigargin) and oxidative stress (rotenone plus oligomycin-A and 6-hydroxydopamine) to evaluate potential neuroprotective compounds.

摘要

牛肾上腺嗜铬细胞的原代培养被认为是评估潜在神经保护化合物的良好模型,主要有两个原因:(i) 它们在合成、储存和释放神经递质方面与神经元有许多共同特征;它们是可兴奋的细胞,表达电压依赖性钙、钾和钠通道;它们表达不同的神经元受体亚型;(ii) 它们可以很容易地从成年动物中大量培养;作为成年副神经元,它们可以用于复制不同的神经退行性样细胞毒性模型。在这一章中,我们描述了模拟钙超载(藜芦碱和他普西苷)和氧化应激(鱼藤酮加寡霉素 A 和 6-羟多巴胺)的方案,以评估潜在的神经保护化合物。

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